7-substituted quinolones and naphthyridones as antibacterial agents

ABSTRACT

##STR1##   7-Substituted quinolones and naphthyridones are described as antibacterial agents as well as a process for their manufacture, compositions therefor, wherein the 7-substituent is a pyrrolidine ring substituted at the 3-position by a substituted aromatic hydrocarbon or a heteroaromatic group.

This is a divisional of U.S. application Ser. No. 08/221,145 filed Mar.30, 1994, now U.S. Pat. No. 5,384,407, which is a divisional of U.S.application Ser. No. 08/014,286 filed Feb. 5, 1993, now U.S. Pat. No.5,342,844, which is a divisional of U.S. application Ser. No. 07/832,188filed Feb. 6, 1992, now U.S. Pat. No. 5,221,676.

BACKGROUND OF THE INVENTION

The present invention is related to novel 7-substituted quinolones andnaphthyridones which are useful in treating bacterial infections,particularly against gram-positive and gram-negative bacteria. The7-substituent is a pyrrolidine ring substituted at the 3-position by asubstituted aromatic hydrocarbon or a heteroaromatic group.

SUMMARY OF THE INVENTION

Accordingly, the present invention includes 7-substituted quinolones andnaphthyridones of Formula I: ##STR2## wherein * denotes an asymmetriccarbon;

X is C--H, C--F, C--Cl, C--OCH₃, C--CF₃, or N;

R¹ is a C₁ -C₄ -alkyl, C₃ -C₆ -cycloalkyl, or phenyl substituted by oneor more halogen atoms;

R² is hydrogen, alkyl of 1 to 4 carbon atoms, or a cation;

R³ is hydrogen, amino, or methyl;

V, W, Y, and Z are each independently C--H, oxygen, nitrogen, or sulfur;

T is C--H or nitrogen;

n is 0 or 1;

R⁴ is hydrogen or one, two or three substituents independently selectedfrom C₁ -C₄ -alkyl, halo-substituted C₁ -C₄ -alkyl, hydroxy-substitutedC₁ -C₄ -alkyl, halogen, hydroxy, C₁ -C₄ -alkoxy, mercapto, amino,mono-(C₁ -C₄ -alkyl)amino, di-(C₁ -C₄ -alkyl)amino, formamido, mono-(C₁-C₄ -alkyl)amido, di-(C₁ -C₄ -alkyl)amido, cyano, nitro, C₁ -C₄-alkoxycarbonyl, carboxyl, aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl,di-(C₁ -C₄ -alkyl)aminomethyl, wherein free hydroxy and amino groups maybe protected;

with the proviso that when T, V, W, Y, and Z are C--H and n is 1, R⁴ isaminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl or di-(C₁ -C₄-alkyl)aminomethyl,

and their pharmaceutically acceptable acid addition or quaternaryammonium salts thereof, when taken together, V, W, Y, Z, T, and R⁴contain at least one amino or oxygen function capable of acting as aproton acceptor.

The invention also includes a pharmaceutical composition comprising anantibacterially effective amount of a compound according to Formula I ora pharmaceutically acceptable salt thereof, in combination with apharmaceutically acceptable carrier or diluent.

The invention further includes a method for treating bacterialinfections in mammals, which comprises administering an antibacteriallyeffective amount of the above defined pharmaceutical composition to amammal in need thereof.

In another aspect, the invention includes a process for the preparationof a compound of Formula I, which comprises reacting a compound ofFormula II: ##STR3## where L is fluorine, chlorine, or other leavinggroup, and X, R¹, R², and R³ are as defined previously, with apyrrolidine of Formula III: ##STR4## wherein * denotes an asymmetriccarbon and T, V, W, Y, Z, R⁴, and n are as defined previously.

The invention in still another aspect includes a process for thesynthesis of pyrrolidines of Formula IV: ##STR5## wherein * denotes anasymmetric carbon and T, V, W, Y, Z, R⁴, and n are as definedpreviously;

R⁵ is hydrogen or an amino protecting group such as benzyl, (R)-or(S)-1-methylbenzyl, benzyloxycarbonyl, or tert-butoxycarbonyl;comprising:

(a) preparation, by known methods, of a substituted ethylene derivativeof the Formula V;

(b) reaction of the above ethylene derivative with an azomethine ylideof Formula VI: ##STR6##

Certain novel intermediates in the process for preparing compounds ofFormula I are also included in the present invention. They includepyrrolidines of Formula IV as defined above, excluding 2- and 3-pyridylgroups on pyrrolidine.

DETAILED DESCRIPTION AND PREFERRED EMBODIMENTS

Substituents for the compounds of Formula I are hereafter defined:

The C₁ -C₄ -alkyl or alkoxy groups comprise both straight and branchedcarbon chains of one to four carbon atoms and include methyl, propyl,1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, and1,1-dimethylethyl.

The cycloalkyl groups contemplated by the invention comprise thosehaving three to six carbon atoms such as cyclopropyl, cyclobutyl,cyclopentyl, and cyclohexyl.

The hydroxyalkyl groups contemplated by the invention comprise thosehaving two to four carbon atoms such as 2-hydroxyethyl, 2- or3-hydroxypropyl, 2-, 3-, or 4-hydroxybutyl.

The term haloalkyl is intended to include halogen substituted straightand branched carbon chains of from two,to four carbon atoms. Thoseskilled in the art will recognize that the halogen substituents may notbe present on the α-carbon atom of the chain. Representative of suchgroups are β-fluoroethyl, β-chloroethyl, β,β-dichloroethyl,β-chloropropyl, β-chloro-2-propyl, and the like.

The term halogen is intended to include fluorine, chlorine, bromine, andiodine.

T, W, Y, Z, and R⁴ together define the substituent on the 3-position ofthe pyrrolidine ring located at the 7-position of the quinolones andnaphthyridones of Formula I. The groups contemplated at the 3-positionof the pyrrolidine ring are substituted aromatic or heteroaromaticgroups. Substituted aromatic groups are phenyl substituted by R⁴ whereinR⁴ is limited to aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl or di-(C₁-C₄ -alkyl)aminomethyl.

The heteroaromatic groups contemplated by the definition of T, W, Y, Z,n, and substituent R⁴ are 5- or 6-membered unsaturated rings having oneto four heteroatoms selected from nitrogen, oxygen, and sulfur. Theyinclude, for example: 2- and 3-pyrrolyl, 2- and 3-furanyl, 2- and3-thiophenyl, 3-, 4-, and 5-pyrazolyl, 3-, 4-, and 5-isoxazolyl, 3-, 4-,and 5-isothiazolyl, 2-, 4-, and 5-imidazolyl, 2-, 4-, and 5-oxazolyl,2-, 4-, and 5-thiazolyl, 1,3,4-triazol-2-yl, 1,3,4-oxadiazol-2-yl,1,3,4-thiadiazol-2-yl, 1,2,4-triazol-3 (or 5)-yl, 1,2,4-oxadiazol-3(or5)-yl, 1,2,4-thiadiazol-3 (or 5)-yl, 5-tetrazolyl, 3- and 4-pyridazinyl,2-, 4-, and 5-pyrimidinyl, 2-pyrazinyl, and 2-, 3-, and 4-pyridinyl. Theheteroaromatic groups may also be substituted by substituents defined byR⁴ without the limitations as in the aromatic group.

Free hydroxyl and amino groups may be protected by known protectivegroups which are easily removable by hydrolysis or hydrogenolysis.

Groups which protect hydroxy are, for example, benzyl, p-methoxybenzyl,acetyl, tetrahydropyranyl, tert-butyl, 2-chloroethyl, methoxy, methyl,trimethylsilyl, etc.

The groups are attached by reacting the free hydroxy group or its anionwith the appropriate halide (or other electrophile) under conditionsknown in the art.

The protective group may then be easily removed by hydrogenation, oracid-or base-catalyzed hydrolysis.

Groups protecting amino are, for example, benzyl, p-methoxybenzyl,benzyloxycarbonyl, tert-butyloxycarbonyl, acetyl, trifluoroacetyl,trimethylsilyl, etc.

The groups are attached by reacting the free amine with the appropriatehalide, acid chloride or anhydride, carbonate, or chlorocarbonate underconditions known in the art.

The amino protecting group may be easily removed by hydrogenation, ormild acid or base-catalyzed hydrolysis.

Certain compounds of the invention may exist in optically active forms.The pure R isomer, pure S isomer as well as mixtures thereof, includingthe racemic mixtures, are contemplated by the invention. Additionalasymmetric carbon atoms may be present in a substituent such as an alkylgroup. All such isomers as well as mixtures thereof are intended to beincluded in the invention. Certain side chains may contain more than onechiral center. In these cases the diasteroisomers may be separated andutilized individually. All such mixtures and separated mixtures arecontemplated by the invention.

The compounds of the invention are capable of forming bothpharmaceutically acceptable acid addition and/or base salts, wherein R²is a cation. Base salts are formed with metals or amines, such as alkaliand alkaline earth metals or organic amines. Examples of metals used ascations are sodium, potassium, magnesium, calcium, and the like. Alsoincluded are heavy metal salts such as, for example, silver, zinc,cobalt, and cerium. Such heavy metal salts are effective in thetreatment of burns, especially when applied to the affected surface of aburn victim either directly or in combination with a physiologicallyacceptable carrier such as a water dispersible, hydrophilic carrier.Examples of suitable amines are N,N'-dibenzylethylenediamine,chloroprocaine, choline, diethanolamine, ethylenediamine,N-methylglucamine, and procaine.

Pharmaceutically acceptable acid addition salts are formed with organicand inorganic acids.

Examples of suitable acids for salt formation are hydrochloric,sulfuric, phosphoric, acetic, lactic, citric, oxalic, malonic,salicylic, malic, gluconic, fumaric, succinic, ascorbic, maleic,methanesulfonic, and the like. The salts are prepared by contacting thefree base form with a sufficient amount of the desired acid to produceeither a mono or di salt in the conventional manner. The free base formmay be regenerated by treating the salt form with a base. For example,dilute solutions of aqueous base may be utilized. Dilute aqueous sodiumhydroxide, potassium carbonate, ammonia, and sodium bicarbonatesolutions are suitable for this purpose. The free base forms differ fromtheir respective salt forms somewhat in certain physical properties suchas solubility in polar solvents, but the salts are otherwise equivalentto their respective free base forms for purposes of the invention. Useof excess base where R¹ is hydrogen gives the corresponding basic salt.

Certain compounds of the invention are also capable of formingquaternary ammonium salts. These salts are formed by reaction of anavailable nitrogen, e.g., on a heteroaromatic ring, with a C₁ -C₄ -alkylor aralkyl halide, preferably an iodide. Preferred alkyl and aralkylgroups are methyl and benzyl.

The compounds of the invention can exist in unsolvated as well assolvated forms, including hydrated forms. In general, the solvatedforms, including hydrated forms and the like are equivalent to theunsolvated forms for purposes of the invention.

Preferred compounds of the present invention and of Formula I are thosewherein X, R², R³, T, V, W, Y, Z, and n are as defined above; R¹ is C₃-C₆ -cycloalkyl or phenyl substituted by one or more halogen atoms, andR⁴ is hydrogen, hydroxy, C₁ -C₄ -alkoxy, hydroxy substituted C₁ -C₄-alkyl, amino, mono-(C₁ -C₄ -alkyl)amino, di-(C₁ -C₄ -alkyl)amino,aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl or di-(C₁ -C₄ -aminomethyl.

More preferred compounds of Formula I are those wherein R², T, V, W, Y,Z, and n are as defined above; X is C--H, C--F, C--Cl, C--OCH₃, or N; R¹is cyclopropyl or 2,4-difluorophenyl; R³ is hydrogen or amino, and R⁴ ishydrogen, hydroxy, hydroxymethyl, amino, methylamino, dimethylamino,aminomethyl, methylaminomethyl, or dimethylaminomethyl.

As further preferred embodiments for compounds of Formula I, when n is1, V, W, Y, and Z are each C--H, T is C--H or N or at least one of V, W,Y, or Z is N; when n is O, V is C--H, N, O or S; Y is C--H, N or S, andW and Z are each independently C--H or N.

Still more preferred compounds of this invention and of Formula I arethose wherein R² is hydrogen or a cation; T, V, W, Y, Z, and n whentaken together form an aromatic or heteroaromatic ring selected from thegroup consisting of 2-and 3-pyrrolyl, 2- and 3-furanyl, 2- and3-thiophenyl, 3-, 4- and 5-pyrazolyl, 2-, 4-, and 5-thiazolyl,1,3,4-oxadiazol-2-yl, 1,2,4-oxadiazol-3(or 5)-yl, 1,2,4-thiadiazol-3(or5)-yl, 1,3,4-thiadiazol-2-yl, 2-, 4-, and 5-pyrimidinyl, 2-pyrazinyl,2-, 3-, 4-pyridinyl, and phenyl; X is C--H, C--F, C--Cl, C--OCH₃, or N;R¹ is cyclopropyl or 2,4-difluorophenyl; R³ is hydrogen or amino, and R⁴i s hydrogen, hydroxy, hydroxymethyl, amino, methylamino, dimethylamino,aminomethyl, methylaminomethyl, or dimethylaminomethyl, with the sameproviso that when T, V, W, Y, Z, and n are taken together to form aphenyl ring, R⁴ is aminomethyl, methylaminomethyl, ordimethylaminomethyl.

Most preferred compounds of Formula I are those wherein R² is hydrogenor a cation; T, V, W, Y, Z, and n when taken together form an aromaticor heteroaromatic ring selected from 2- and 3-pyrrolyl, 2- and3-furanyl-, 2- and 3-thiophenyl, 3-, 4-, and 5-pyrazolyl,1,2,4-oxadiazol-3(or 5)-yl, 2-, 3-, and 4-pyridinyl, and phenyl; X isC--H, C--F, C--Cl, C--OCH₃, or N; R¹ is cyclopropyl or2,4-difluorophenyl; R³ is hydrogen or amino, and R⁴ i s hydrogen,hydroxy, hydroxymethyl, amino, or aminomethyl, with the same provisothat when T, V, W, Y, Z, and n are taken together to form a phenyl ring,R⁴ is aminomethyl.

Particularly valuable compounds of Formula I are

7-[3-[2-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

7-[3-[2-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[2-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

7-[3-[2-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid;

b7-[3-[3-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

7-[3-[3-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[3-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

7-[3-[4-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

7-[3-[4-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[4-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-7-[3-[3-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-[4-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-7-[3-[4-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-[4-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid;

7-[3-(3-amino-2-pyridinyl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

7-[3-[3-(aminomethyl)-2-pyridinyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[3-(aminomethyl)-2-pyridinyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-oxo-3-quinolinecarboxylicacid;

1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid;

7-[3-[3-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylicacid;

7-[3-[2-(aminomethyl)-1H-imidazol-4-yl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-5-methyl-4-oxo-3-quinolinecarboxylicacid;

7-[3-[2-(aminomethyl)-4-thiazolyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

7-[3-(5-amino-4-thiazolyl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-[4-(hydroxymethyl)-2-thiazolyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

5-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-(1H-imidazol-2-yl)-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid;

7-[3-(3-amino-1,2,4-oxadiazol-5-yl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

5-amino-7-[3-(4-amino-2-thiazolyl)-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[3-(aminomethyl)-1,2,4-oxadiazol-5-yl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

5-amino-7-[3-[3-(aminomethyl)-1H-1,2,4-triazol-5-yl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

7-[3-(5-amino-1,3,4-oxadiazol-2-yl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid;

7-[3-(3-amino-1H-1,2,4-triazol-5-yl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid;

1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyrimidinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid;

1-cyclopropyl]-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-pyrimidinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid, and

5-amino-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-7-[3-(2-pyrazinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid.

The compounds of the present invention and of Formula I, as well asintermediates of Formula III, may be prepared generally as describedabove.

Particularly, the compounds of Formula I may be prepared, for example,as illustrated by the following reaction schemes. ##STR7##

Starting from a vinylbenzene derivative or any vinylheteroaromaticderivative (Scheme I), which is commercially available or can beprepared by known literature procedures, conversion to the correspondingN-protected-3-substituted pyrrolidine is preferably done by reactionwith N-benzyl-N-(methoxymethyl)trimethylsilylmethylamine and a catalyticamount of trifluoroacetic acid in dichloromethane at -10° C. to thereflux temperature of the reaction mixture, and for 0.5 to 12 hours.Other solvents include acetonitrile, tetrahydrofuran, dioxane,chloroform, dichloroethane, toluene, and the like. Alternative catalystsinclude anhydrous potassium or cesium fluoride, tetra-n-butylammoniumfluoride, trifluoromethanesulfonic acid, trimethylsilyltrifluoromethanesulfonate, and iodotrimethylsilane [cf. A. Hosomi, etal, Chem. Lett. 1117 (1984); Y. Terao, et al, Chem. Pharm. Bull. 33:2762(1985)].

Reduction of the nitro or cyano substituents is best accomplished bycatalytic hydrogenation with hydrogen gas. The preferred catalystsinclude Raney nickel and varying percentages of rhodium, platinum, orplatinum oxide on an inert support such as carbon or alumina. Methanol,ethanol, tetrahydrofuran, acetic acid, and ethyl acetate, with orwithout the addition of water, ammonia, or hydrochloric acid, are usedas solvent. The reaction is run at ambient temperature to 80°-90° C. for0.5 to 24 hours. Alternatively, the reduction can be carried forwardwith a hydride reducing agent in an inert solvent. The preferred methodemploys lithium aluminum hydride in tetrahydrofuran at reflux for 2 to12 hours.

The resulting amino or aminomethyl substituent may be reacted with anamino-protecting reagent such as acetic anhydride, acetyl chloride,trifluoroacetic anhydride, methyl trifluoroacetate, or di-tert-butyldicarbonate, in the presence of a tertiary amine such as triethylamine,diisopropylethylamine, or pyridine, with or without an inert solventsuch as an ether or chlorocarbon, in a temperature range of 0° C. to thereflux temperature of the reaction mixture, and for 6 to 72 hours.Preferred conditions are with di-tert-butyl dicarbonate anddiisopropylethylamine in dichloromethane at room temperature for 12hours.

The N-acetyl-, N-trifluoroacetyl-, or N-tert-butoxycarbonyl-protectedcompounds may be reacted with a proton abstractor such as sodium hydrideor a similar agent, in a solvent such as tetrahydrofuran ordimethylformamide, at -20° C. to 80° C., followed by addition of amethylating agent like iodomethane or methyl trifluoromethanesulfonate,to give the corresponding N-methylated derivative. The trifluoroacetylor tert-butoxycarbonyl group may be removed by acid-or base-catalyzedhydrolysis, preferably with sodium hydroxide or trifluoroacetic acid,respectively. Alternatively, the N-acetyl orN-tert-butoxycarbonyl-protected compound may be reacted directly with ahydride reducing agent in an inert solvent, preferably lithium aluminumhydride in tetrahydrofuran, at 25° C. to the reflux temperature of themixture, for 1 to 20 hours, to afford the corresponding N-ethyl orN-methyl substituted derivative, respectively.

The compounds bearing an unprotected amino or aminomethyl group may alsobe dimethylated by reaction with aqueous formaldehyde in formic acid, at0° C. to the reflux temperature of the reaction mixture, for 2 to 10hours.

The above derivatives, whether bearing an amino-protecting group or not,are debenzylated via hydrogenolysis with hydrogen gas or a source ofhydrogen such as ammonium formate, cyclohexene, or cyclohexadiene, usingvarying percentages of palladium on an inert support such as carbon,alumina, silica, or the like, preferably 20% palladium on carbon, in aninert solvent such as methanol, ethanol, tetrahydrofuran, acetic acid,or ethyl acetate, with or without the addition of hydrochloric acid.Alternatively, a non-hydrogenolytic debenzylation can be carried outconsisting in reacting the N-benzyl derivative with a silyl-substitutedchloro-or azidoformate, followed by treatment of the resulting carbamatewith a desylating agent, such as a source of fluoride ion. This providesthe corresponding 3-(aminomethylphenyl or pyridyl)pyrrolidines in a formsuitable for coupling with a quinolone or naphthyridine substrate ofFormula II.

DESCRIPTION OF SCHEME II

Alternatively, starting with a suitably N-protected-3-alkoxycarbonylsubstituted pyrrolidine (Scheme II), conversion to a3-(1,2,4-oxadiazol-5-yl) pyrrolidine may be accomplished by reactionwith acetamide oxime or hydroxyguanidine sulfate, in the presence of aproton abstractor such as a metal hydride, sodium or potassium alkoxide,or sodium metal, in a solvent such as benzene, toluene, diethyl ether,tetrahydrofuran, diglyme, methanol, or ethanol, at 25° C. to the refluxtemperature of the reaction mixture. Preferred conditions include sodiumhydride in tetrahydrofuran at reflux or sodium metal in ethanol atreflux. Alternatively, reaction with aminoguanidine bicarbonate providesthe corresponding 3-(1,2,4-triazol-5-yl)substituted pyrrolidine.

The 3-alkoxycarbonyl substituted pyrrolidine can be directly convertedinto other 3-heteroaryl substituted pyrrolidines using known art. Thistransformation may also be carried out via the corresponding carboxylicacid, available by selective hydrolysis of the ester with varyingconcentrations of sodium or potassium hydroxide in a water-alcoholmixture, at a temperature ranging from -10° C. to room temperature. Theresulting acid can then be converted into the corresponding acidchloride by established literature procedures, for instance, by reactionwith oxalyl chloride in dichloromethane at room temperature and in thepresence of a catalytic amount of dimethylformamide. Treatment of theacid chloride with a substituted hydrazide, semicarbazide, orthiosemicarbazide, followed by ring closure under base-oracid-catalysis, affords the corresponding 3-heteroaryl substitutedpyrrolidines.

The compounds of the invention display antibacterial activity whentested by the microtitration dilution method as described in Heifetz, etal, Antimicr. Agents & Chemoth. 6:124 (1974), which is incorporatedherein by reference.

By use of the above reference method, the following minimum inhibitoryconcentration value (MICs in μg/mL)shown in Table I were obtained forrepresentative compounds of the invention.

                                      TABLE I                                     __________________________________________________________________________    In Vitro Antibacterial Activity                                               Minimal Inhibitory Concentration MIC (μg/mL)                               Example                                                                            Enter.                                                                            E. coli                                                                           Kleb.                                                                            Prot.                                                                            Pneu.                                                                             S. aureus                                                                             Streptococcus                                  No.  cloac.                                                                            Vogel                                                                             pneu.                                                                            rettg.                                                                           aeru.                                                                             R  S    faec.                                                                            pneum.                                                                             pyog.                                  __________________________________________________________________________     1   0.1 0.1 0.2                                                                              0.4                                                                              1.6 0.05                                                                             0.013                                                                              0.05                                                                             0.025                                                                              0.025                                   6   0.05                                                                              0.05                                                                              0.05                                                                             0.1                                                                              0.8 0.013                                                                            0.006                                                                              0.025                                                                            0.006                                                                              0.006                                   7   0.05                                                                              0.05                                                                              0.1                                                                              0.1                                                                              0.8 0.025                                                                            0.006                                                                              0.013                                                                            ≦0.003                                                                      ≦0.003                           8   0.05                                                                              0.05                                                                              0.1                                                                              0.2                                                                              0.8 0.013                                                                            ≦0.003                                                                      0.013                                                                            0.006                                                                              0.013                                  11   0.1 0.1 0.2                                                                              0.2                                                                              0.8 0.013                                                                            ≦0.003                                                                      0.013                                                                            0.013                                                                              0.013                                  13   0.2 0.2 0.4                                                                              0.8                                                                              1.6 0.05                                                                             0.013                                                                              0.05                                                                             0.05 0.05                                   14   0.2 0.2 0.4                                                                              0.4                                                                              1.6 0.013                                                                            0.006                                                                              0.025                                                                            0.013                                                                              0.013                                  15   0.2 0.2 0.4                                                                              0.4                                                                              1.6 0.013                                                                            0.006                                                                              0.025                                                                            0.013                                                                              0.013                                  17   0.1 0.1 0.2                                                                              0.2                                                                              0.8 0.006                                                                            ≦0.003                                                                      0.05                                                                             0.05 0.05                                   21   0.1 0.1 0.2                                                                              0.2                                                                              0.8 0.006                                                                            ≦0.003                                                                      0.025                                                                            0.025                                                                              0.025                                  22   0.1 0.1 0.2                                                                              0.2                                                                              1.6 0.006                                                                            ≦0.003                                                                      0.05                                                                             0.025                                                                              0.025                                  25   0.2 0.2 0.4                                                                              0.4                                                                              3.1 0.006                                                                            ≦0.003                                                                      0.05                                                                             0.05 0.05                                   29   0.05                                                                              0.05                                                                              0.1                                                                              0.2                                                                              1.6 0.025                                                                            0.013                                                                              0.025                                                                            0.025                                                                              0.025                                  __________________________________________________________________________

The compounds of the invention can be prepared and administered in awide variety of oral, parenteral, and topical dosage forms. It will beobvious to those skilled in the art that the following dosage forms maycomprise as the active component, either a compound of Formula I or acorresponding pharmaceutically acceptable salt of a compound of FormulaI.

For preparing pharmaceutical compositions from the compounds describedby this invention, inert, pharmaceutically acceptable carriers can beeither solid or liquid. Solid form preparations include powders,tablets, dispersible granules, capsules, cachets, suppositories, andointments. A solid carrier can be one or more substances which may alsoact as diluents, flavoring agents, solubilizers, lubricants, suspendingagents, binders, or tablet disintegrating agents; it can also be anencapsulating material. In powders, the carrier is a finely dividedsolid which is in admixture with the finely divided active compound. Inthe tablet the active compound is mixed with carrier having thenecessary binding properties in suitable proportions and compacted inthe shape and size desired. The powders and tablets preferably containfrom 5 to 10 to about 70 percent of the active ingredient. Suitablesolid carriers are magnesium carbonate, magnesium stearate, talc, sugar,lactose, pectin, dextrin, starch, gelatin, tragacanth, methyl cellulose,sodium carboxymethyl cellulose, a low melting wax, cocoa butter, and thelike. The term "preparation" is intended to include the formulation ofthe active compound with encapsulating material as carrier providing acapsule in which the active component (with or without other carriers)issurrounded by carrier, which is thus in association with it. Similarly,cachets are included. Tablets, powders, cachets, and capsules can beused as solid dosage forms suitable for oral administration.

Liquid form preparations include solutions, suspensions, and emulsions.As an example may be mentioned water or water-propylene glycol solutionsfor parenteral injection. Such solutions are prepared so as to beacceptable to biological systems (isotonicity, pH, etc). Liquidpreparation can also be formulated in solution in aqueous polyethyleneglycol solution. Aqueous solutions suitable for oral use can be preparedby dissolving the active component in water and adding suitablecolorants, flavors, stabilizing, and thickening agents as desired.Aqueous suspension suitable for oral use can be made by dispersing thefinely divided active component in water with viscous material, i.e.,natural or synthetic gums, resins, methyl cellulose, sodiumcarboxymethyl cellulose, and other well-known suspending agents.

Ointment preparations contain heavy metal salts of a compound of FormulaI with a physiologically acceptable carrier. The carrier is desirably aconventional water-dispersible hydrophilic or oil-in-water carrier,particularly a conventional semi-soft or cream-like water-dispersible orwater soluble, oil-in-water emulsion which may be applied to an affectedburn surface or infected surface with a minimum of discomfort. Suitablecompositions may be prepared by merely incorporating or homogeneouslyadmixing finely divided compounds with the hydrophilic carrier or baseor ointment.

Preferably, the pharmaceutical preparation is in unit dosage form. Insuch form, the preparation is subdivided into unit doses containingappropriate quantities of the active component. The unit dosage form canbe a packaged preparation, the package containing discrete quantities ofpreparation, for example, packeted tablets, capsules, powders in vialsor ampules, and ointments in tubes or jars. The unit dosage form canalso be a capsule, cachet, tablet, gel or cream itself or it can be theappropriate number of any of these packaged forms.

The quantity of active compound in a unit dose of preparation may bevaried or adjusted from 1 mg to 100 mg according to the particularapplication and the potency of the active ingredient.

In therapeutic use as agents for treating bacterial infections thecompounds utilized in the pharmaceutical method of this invention areadministered at the initial dosage of about 3 mg to about 40 mg perkilogram daily. A daily dose range of about 6 mg to about 14 mg perkilogram is preferred. The dosages, however, may be varied dependingupon the requirements of the patient, the severity of the conditionbeing treated, and the compound being employed. Determination of theproper dosage for a particular situation is with the skill of the art.Generally, treatment is initiated with smaller dosages which are lessthan the optimum dose of the compound. Thereafter, the dosage isincreased by small increments until the optimum effect under thecircumstances is reached. For convenience, the total daily dosage may bedivided and administered in portions during the day if desired.

The following nonlimiting examples illustrate methods for preparing thecompounds of the invention.

PREPARATION OF STARTING PYRROLIDINES EXAMPLE A

2-[1-(Phenylmethyl)-3-pyrrolidinyl]benzonitrile

A solution of N-benzyl-N-(methoxymethyl)trimethylsilylmethylamine (16.62g,70.0 mmol) in dichloromethane (15 mL) are added dropwise, over a45-minute period, to a solution of 2-ethenylbenzonitrile (6.00 g, 46.0retool) and trifluoroacetic acid (0.57 g, 5.0 retool) in dichloromethane(55 mL). The resulting solution was stirred at room temperature for anadditional 10 to15 minutes, and then heated with saturated aqueoussodium bicarbonate solution (ca 10-15 mL). The organic layer wasdecanted, washed with water,and dried over anhydrous magnesium sulfate.Filtration and concentration ofthe solution provided an orange oil whichwas chromatographed (silica-gel, hexanes-ethyl acetate 5:1) to affordthe title compound (6.95 g, 58%) as apale yellow oil. ¹ H-NMR (300 MHz,CDCl₃): δ=1.80-1.92 (1H,m), 2.43-2.55 (1H, m), 2.63-2.75 (2H, m),2.88-2.96 (2H, m), 3.71 (2H, AB quartet, J_(AB) =13.0 Hz), 3.78-3.86(1H, m), 7.25-7.41 (6H, m), 7.53-7.66 (3H, m).

EXAMPLE B

3-[1-(Phenylmethyl)-3-pyrrolidinyl]benzonitrile

Starting from 3-ethenylbenzonitrile (8.00 g, 62.0 mmol), a procedureanalogous to that given in Example A provided the title compound (12.41g,76%) as a faint yellow oil after chromatography (silica gel,hexanes-ethyl acetate 2: 1).

¹ H-NMR (250 MHz, CDCl₃): δ=1.75-1.89 (1H, m), 2.29-2.44 (1H, m), 2.54(1H, dd, J=9.3, 6.5 Hz), 2.67-2.84 (2H, m), 2.93 (1H, dd, J=9.3, 7.7Hz), 3.30-3.42 (1H, m), 3.67 (2H, AB quartet, J_(AB) =13.2 Hz),7.22-7.39 (6H, m), 7.45-7.54 (2H, m), 7.58-7.59 (1H, m).

EXAMPLE C

4-[1-(Phenylmethyl)-3-pyrrolidinyl]benzonitrile

Starting from 4-ethenylbenzonitrile (8.80 g, 68.1 mmol), a procedureanalogous to that given in Example A provided the title compound (13.59g,76%) as an off-yellow solid after recrystallization from ethylacetate/hexanes, mp 78°-79° C.

¹ H-NMR (250 MHz, CDCl₃): δ=1.79-1.92 (1H, m), 2.30-2.45 (1H, m),2.56-2.62 (1H, m), 2.70-2.85 (2H, m), 2.96 (1H, dd, J=9.4, 7.9 Hz),3.34-3.44 (1H, m), 3.69 (2H, s), 7.25-7.41 (7H, m), 7.55-7.59 (2H, m).

EXAMPLE D

2-[1-(Phenylmethyl)-3-pyrrolidinyl]pyridine

Starting from 2-ethenylpyridine (7.00 g, 66.6 mmol), a procedureanalogous to that given in Example A provided the title compound (12.50g, 79%) as alight orange oil after chromatography (silica gel,chloroform-methanol 20:1).

¹ H-NMR (250 MHz, CDCl₃): δ=2.03-2.16 (1H, m), 2.27-2.41 (1H, m), 2.65(1H, dd, J=9.2, 7.9 Hz), 2.69-2.76 (1H, m), 2.83-2.92 (1H, m), 3.08 (1H,dd, J=8.6, 7.9 Hz), 3.48-3.64 (1H, m), 3.69 (2H, s), 7.05-7.11 (1H, m),7.16-7.38 (6H, m), 7.54-7.61 (1H, m), 8.53 (1H, d, J=4.9 Hz).

EXAMPLE E

3-[1-(Phenylmethyl)-3-pyrrolidinyl]pyridine

Starting from 3-ethenylpyridine (6.2 0 g, 59.0 mmol), a procedureanalogousto that given in Example A provided the title compound (5.10 g,36%) as an orange oil after chromatography (silica gel,chloroform-methanol 20:1).

¹ H-NMR (250 MHz, CDCl₃): δ=1.80-1.94 (1H, m), 2.31-2.45 (1H, m), 2.58(1H, dd, J=9.1, 7.0 Hz), 2.76-2.82 (2H, m), 2.96-3.03 (1H, m), 3.31-3.43(1H, m), 3.70 (2H, s), 7.19-7.38 (6H, m), 7.64 (1H, dist. d,J=7.9 Hz),8.43 (1H, d, J=4.7 Hz), 8.51 (1H, dist. d, J=2.1 Hz).

EXAMPLE F

4-[1-(Phenylmethyl)-3-pyrrolidinyl]pyridine

Starting from 4-ethenylpyridine (4.21 g, 40.0 mmol), a procedureanalogous to that given in Example A provided the title compound (6.50g, 68%) as a yellow oil after chromatography (silica gel,chloroform-methanol 20:1).

¹ H-NMR (250 Hz, d₆ -DMSO): δ1.68-1.82 (1H, m), 2.19-2.33 (1H, m), 2.48(1H, dd, J=9.1, 6.5 Hz), 2.61 (1H, dd, J=16.0, 8.7 Hz), 2.66-2.76 (1H,m), 2.85 (1H, dist. t, J=8.6, 8.2 Hz), 3.26-3.38 (1H, m), 3.63 (2H, ABquartet, J_(AB) =13.1 Hz), 7.22-7.34 (7H, m), 8.45 (2H, d, J=5.4 Hz).

EXAMPLE G

3-Nitro-2-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine

Starting from 2-ethenyl-3-nitropyridine (4.50 g, 30.0 mmol), a procedureanalogous to that given in Example A provided the title compound (5.50g, 65%) as a yellow oil after chromatography (silica gel, hexanes-ethylacetate 1:1).

¹ H-NMR (300 MHz, CDCl₃): δ=2.20-2.45 (2H, m), 2.78-3.00 (3H, m),3.15-3.27 (1H, m), 3.60-3.89 (2H, m), 4.02-4.11 (1H, m), 7.20-7.70 (6H,m), 8.08 (1H, dd, J=8.3, 1.7 Hz), 8.80 (1H, dd, J=4.8, 1.7 Hz).

EXAMPLE H

2-[1-(Phenylmethyl-3-pyrrolidinyl]-3-pyridinecarbonitrile

Starting from 2-ethenyl-3-pyridinecarbonitrile (3.90 g, 30.0 mmol), aprocedure analogous to that given in Example A provided the titlecompound(4.78 g, 54%) as a yellow oil after chromatography (silica gel,hexanes-ethyl acetate 1:1).

¹ H-NMR (300 MHz, CDCl₃): δ=2.15-2.37 (1H, m), 2.32-2.46 (1H, m),2.70-2.81 (2H, m), 2.90-3.00 (1H, m), 3.17 (1H, t, J=8.6 Hz), 3.74 (2H,AB quartet, J_(AB) =12.9 Hz), 3.98-4.09 (1H, m), 7.21-7.41 (6H, m), 7.88(1H, dd, J=7.9, 1.8 Hz), 8.77 (1H, dd, J=4.9, 1.7 Hz).

EXAMPLE I

3-[1-(Phenylmethyl)-3-pyrrolidinyl]benzenemethanamine

A suspension of 3-[1-(phenylmethyl)-3-pyrrolidinyl]benzonitrile (11.90g, 45.4 mmol) and Raney nickel (5.0 g) in methanol saturated withammonia (100 mL) was hydrogenated in a Parr shaker at 3 atm. Theresulting suspension was filtered through a pad of Celite and thefiltrate concentrated to give an off-green liquid. This crude productwas chromatographed (silica gel, chloroform-methanol 2:1) to give thetitle compound (10.12 g, 84%) as a colorless oil. ¹ H-NMR (250 MHz,CDCl₃): δ=1.68-1.75 (2H, br. s), 1.83-1.97 (1H, m), 2.27-2.41 (1H, m),2.51 (1H, dd, J=9.0, 8.1 Hz), 2.71 (1H, td, J=8.9, 5.9 Hz), 2.80-2.90(1H, m), 3.01-3.08 (1H, m), 3.31-3.41 (1H, m), 3.69 (2H, AB quartet,J_(AB) =13.3 Hz), 3.84 (2H, s), 7.11-7.39 (9H, m).

EXAMPLE J

4-[1-(Phenylmethyl)-3-pyrrolidinyl]benzenemethanamine

Starting from 4-[1-(phenylmethyl)-3-pyrrolidinyl]benzonitrile (8.28 g,31.6retool), a procedure analogous to that given in Example I providedthe title compound (8.42 g, 100%) as a yellow oil.

¹ H-NMR (250 MHz, CDCl₃): δ=1.79-1.93 (1H, m), 2.00-2.15 (1H, m),2.24-2.39 (2H, m), 2.48 (1H, dd, J=8.9, 8.1 Hz), 2.68 (1H, td, J=8.9,5.9 Hz), 2.78-2.88 (1H, m), 3.02 (1H, dd, J=9.0, 8.0 Hz), 3.35 (1H,dt,J=17.3, 7.7, 7.5 Hz), 3.67 (2H, AB quartet, J_(AB) =13.3 Hz), 3.81 (2H,s), 7.21-7.38 (9H, m).

EXAMPLE K

1,1-Dimethylethyl[[3-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate

A solution of 3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine(8.00 g, 30.0 retool), di-tert-butyl dicarbonate (7.86 g, 36.0 mmol) anddiisopropylethylamine (4.65 g, 36.0 mmol) in dichloromethane (300 mL)was stirred at room temperature for 18 hours. The solvent was removedand the residue was chromatographed (hexanes-ethyl acetate 1:1) to givethe title compound (9.50 g, 86%) as a colorless oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.47 (9H, s), 1.83-1.95 (1H, m), 2.23-2.40(1H, m), 2.50 (1H, dd, J=9.0, 8.2 Hz), 2.72 (1H, td, J=9.0, 6.0 Hz),2.83-2.91 (1H, m), 3.05 (1H, dd, J=9.2, 7.9 Hz), 3.37 (1H, dt, J=17.4,7.7, 7.7 Hz), 3.70 (2H, s), 4.25-4.33 (2H, m), 4.82-4.95 (1H, br. s),7.09-7.39 (9H, m).

EXAMPLE L

1,1-Dimethylethyl[[4-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate

Starting from 4-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine(8.00 g, 30.0 mmol), a procedure analogous to that given in Example Kprovided the title compound (9.80 g, 89%) as a faint yellow oil.

¹ H-NMR (250 MHz, CDCl₃): δ=1.46 (9H, s), 1.79-1.90 (1H, m), 2.23-2.39(1H, m), 2.47 (1H, dd, J=8.9, 8.0 Hz), 2.69 (1H, td, J=8.8, 5.9 Hz),2.77-2.87 (1H, m), 3.01 (1H, dd, J=8.9, 8.0 Hz), 3.27-3.41 (1H, m), 3.66(2H, s), 4.25-4.28 (2H, m), 4.78-4.83 (1H, m), 7.17-7.37 (9H, m).

EXAMPLE M

2-(3-Pyrrolidinyl)benzenemethanamine

A suspension of 2-[1-(phenylmethyl)-3-pyrrolidinyl]benzonitrile (6.98 g,26.6 mmol), 20% palladium on charcoal catalyst (4.0 g), and concentratedhydrochloric acid (4.6 mL) in methanol (200 mL) was hydrogenated in aParrapparatus at 3 atm. The suspension was then filtered through a padof Celite and the filtrate concentrated to give the dihydrochloride saltof the title compound (6.40 g, 97%) as an off-white solid.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.86-1.97 (1H, m), 2.32-2.42(1H, m),2.97-3.08 (1H, m), 3.10-3.23 (1H, m), 3.35-3.42 (1H, m), 3.59-3.74(2H,m), 4.08-4.16 (2H, m), 7.30-7.60 (4H, m), 8.50-8.65 (3H, m),9.44-9.60(1H, m), 9.70-9.85 (1H, m).

EXAMPLE N

1,1-Dimethylethyl[[3(3-pyrrolidinyl)phenyl]methyl]carbamate

A suspension of1,1-dimethylethyl[[3-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate(4.50 g, 12.3 retool) and 20% palladium on charcoal catalyst (0.30 g) inmethanol (100 mL) was hydrogenated in a Parr apparatus at 3 atm. Thesuspension was filtered through a pad of Celite and the filtrateconcentrated to give an orange oil. This oil was chromatographed (silicagel, dichloromethanemethanol 1:1 containing 1% ammonia) to give thetitle compound (2.99 g, 88%) as a pale yellow oil.

¹ H-NMR (250 MHz, CDCl₃): δ=1.46 (9H, s), 1.80-1.93 (1H, m), 2.19-2.35(1H, m), 2.86 (1H, dd, J=10.5, 8.2 Hz), 3.05-3.29 (3H, m), 3.38 (1H, dd,J=10.5, 7.7 Hz), 4.26-4.32 (2H, m), 4.80-4.94 (1H, m), 7.13-7.18 (3H,m), 7.23-7.32 (1H, m).

EXAMPLE O 1,1-Dimethylethyl[[4-(3-pyrrolidinyl)phenyl]methyl]carbamate

Starting from1,1-dimethylethyl[[4-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate(5.17 g, 14.1 retool), a procedure analogous to that given in ExampleNprovided the title compound (3.47 g, 89%) as a pale yellow oil.

¹ H-NMR (250 MHz, CDCl₃): δ=1.46 (9H, s), 1.78-1.91 (1H, m), 2.19-2.27(1H, m), 2.83 (1H, dd, J=10.4, 8.2 Hz), 3.04-3.28 (3H, m), 3.36 (1H, dd,J=10.4, 7.6 Hz), 4.26-4.30 (2H, m), 4.80-4.90 (1H, m), 7.19-7.22 (4H,m).

EXAMPLE P

N-Methyl-3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine

A solution of1,1-dimethylethyl[[3-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate(4.50 g, 12.3 retool), in anhydrous tetrahydrofuran (100 mL) was addedportionwise to a stirred suspension of lithium aluminum hydride (1.28 g,34.0 retool) in dry tetrahydrofuran (100 mL). The resulting suspensionwasheated at reflux for 4 hours, then allowed to cool to roomtemperature, andquenched by addition of saturated aqueous ammoniumsulfate solution (50 mL)and water (100 mL). The precipitated solids werefiltered through a pad of Celite, washed with methanol, and the filtrateand washings concentrated under reduced pressure. The residue was takenup in water and extracted with dichloromethane (4×50 mL). The organicextracts were combined, washed with brine, dried over anhydrousmagnesium sulfate, filtered, and concentrated to an orange oil. This oilwas redissolved in dichloromethaneand treated with hydrogen chloride for30-60 min. Evaporation of the solvent gave an oil which waschromatographed (silica gel, dichloromethane-methanol 5:1) to give thehydrochloride salt (ca. 4.00 g, 100%) of the title compound as a lightorange oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.86-1.97 (1H, m), 2.05-2.14 (1H, m),2.29-2.41 (1H, m), 2.47-2.54 (1H, m), 2.48 (3H, s), 2.66-2.75 (1H, m),2.82-2.90 (1H, m), 3.06 (1H, dd, J=9.0, 7.9 Hz), 3.33-3.43 (1H, m), 3.70(2H, s), 7.75 (2H, s), 7.15-7.40 (9H, m).

EXAMPLE Q

N-Methyl-4-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine

Starting from1,1-dimethylethyl[[4-[1-(phenylmethyl)-3-pyrrolidinyl]phenyl]methyl]carbamate(5.15 g, 14.0. mmol), a procedure analogous to that given in Example Pprovided the title compound (4.07 g, 92%) as an off-white solid.

¹ H-NMR (300 MHz, CDCl₃): δ=1.81-1.92 (1H, m), 2.27-2.38 (1H, m), 2.45(3H, s), 2.46-2.53 (1H, m), 2.66-2.74 (1H, m), 2.79-2.88 (1H, m),2.99-3.04 (1H, m), 3.30-3.41 (1H, m), 3.68 (2H, s), 3.77 (2H,s),4.02-4.11 (1H, br. s), 7.23-7.38 (9H, m).

EXAMPLE R

N-Methyl-3-(3-pyrrolidinyl)benzenemethanamine

Starting fromN-methyl-3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine (4.43 g,15.8 mmol), a procedure analogous to that given in Example M providedthe title compound (1.39 g, 46%) as a pale yellow oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.79-1.91 (1H, m), 2.17-2.28 (1H, m), 2.41(3H, s), 2.82-2.90 (1H, m), 3.04-3.28 (3H, m), 3.32-3.39 (1H, m), 3.68(2H, s), 7.08-7.27 (4H, m).

EXAMPLE S

N-Methyl-4-(3-pyrrolidinyl)benzenemethanamine

Starting fromN-methyl-4-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine (3.96 g,14.1 retool), a procedure analogous to that given in Example M providedthe title compound (1.61 g, 60%) as a pale yellow oil.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.60-1.75 (1H, m), 2.08-2.21(1H, m), 2.22(3H, s), 2.56-2.63 (1H, m), 2.83-3.04 (2H, m), 3.07-3.22 (2H,m), 3.56(2H, s), 7.18-7.25 (4H, m).

EXAMPLE T

N,N-Dimethyl-3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine

A solution of 3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine(1.65 g, 6.2 mmol), sodium formate (1.70 g, 25.0 mmol), 37% aqueousformaldehyde(62 mL) and 90% aqueous formic acid (62 mL) was heated atreflux for 3.5 hours. The solvent was evaporated to give a mixture of awhite solid and ayellow liquid. The solid was filtered and washed withmethanol and ether. The filtrate and washings were combined andconcentrated under reduced pressure. The resulting residue was taken upin water (30 mL), and the solution was made basic with concentratedammonia and extracted with dichloromethane (3×50 mL). The organicextracts were washed with water, dried over anhydrous magnesium sulfate,and concentrated to a yellow oil. This oil was chromatographed (silicagel, dichloromethane-methanol 10:1) to give the title compound (1.35 g,74%) asa colorless oil.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.67-1.80 (1H, m), 2.12 (6H,s), 2.18-2.30(1H, m), 2.43 (1H, dd, J=9.0, 7.1 Hz), 2.63-2.69 (2H, m), 2.86 (1H, dd,J=9.0, 8.0 Hz), 3.23-3.33 (1H, m), 3.34 (2H, s), 3.63 (2H, AB quartet,J_(AB) =13.0 Hz), 7.05-7.09 (1H, m), 7.13-7.33 (8H, m).

EXAMPLE U

N,N-Dimethyl-3-(3-pyrrolidinyl)benzenemethanamine

Starting fromN,N-dimethyl-3-[1-(phenylmethyl)-3-pyrrolidinyl]benzenemethanamine (1.33g, 4.5 mmol), a procedure analogous to that given in Example M providedthe title compound (0.14 g, 15%), as a pale yellow oil.

¹ H-NMR (250 MHz, CDCl₃): δ=1.81-1.92 (1H, m), 2.20-2.29 (1H, m), 2.24(6H, s), 2.89 (1H, dd, J=10.5, 8.3 Hz), 3.07-3.30 (3H, m), 3.36-3.42(3H, m), 7.12-7.29 (4H, m).

EXAMPLE V

2-(3-Pyrrolidinyl)pyridine

To a suspension of 2-[1-(phenylmethyl)-3pyrrolidinyl]pyridine (7.15 g,30.0mmol) and 10% palladium on charcoal catalyst (1.90 g) in methanol(120 mL) was added dropwise a solution of ammonium formate (7.57 g, 120retool) in water (30 mL). The mixture was heated at reflux for 30minutes, allowed tocool to room temperature, and filtered. The filtratewas concentrated underreduced pressure, the residue was taken up inwater (10 mL), and the solution was made basic with concentrated ammoniaand extracted with dichloromethane (4×15 mL). The organic extracts werecombined, driedover anhydrous potassium carbonate, and concentrated to ayellow oil. This crude product was chromatographed (silica gel,chloroform-methanol-ammonia75:25:5) to give the title compound (3.33 g,75%) as a faint yellow liquid.

¹ H-NMR (300 MHz, d₆ -DMSO): δ=1.80-1.92 (1H, m), 2.02-2.13(1H, m),2.75-3.02 (3H, m), 3.11-3.17 (1H, m), 3.22-3.32 (1H, m), 7.16-7.20(1H,m), 7.28 (1H, d, J=7.8 Hz), 7.67 (1H, d, J=7.7 Hz), 8.48 (1H, d,J=4.9Hz).

EXAMPLE W

3-(3-Pyrrolidinyl)pyridine

Starting from 3-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine (5.00 g, 21.0retool), a procedure analogous to that described in Example V providedthetitle compound (2.15 g, 69%) as a pale orange oil.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.60-1.75 (1H, m), 2.08-2.29(1H, m),2.58-2.69 (1H, m), 2.85-3.04 (2H, m), 3.07-3.36 (2H, m), 7.31 (1H,dd,J=7.9, 4.9 Hz), 7.69 (1H, d, J=7.9 Hz), 8.39 (1H, d, J=4.9 Hz), 8.48(1H, s).

EXAMPLE X

4-(3-Pyrrolidinyl)pyridine

Starting from 4-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine (5.90 g, 24.7retool), a procedure analogous to that described in Example V providedthetitle compound (3.00 g, 66%) as an orange oil.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.86-2.02 (1H, m), 2.36-2.45(1H, m),3.09-3.23 (2H, m), 3.35-3.49 (1H, m), 3.53-3.68 (2H, m), 7.51 (2H,d,J=5.9 Hz), 8.58 (2H, d, J=5.9 Hz), 9.80-10.00 (2H, m).

EXAMPLE Y

2-(3-Pyrrolidinyl)-3-pyridinamine

Starting from 3-nitro-2-[1-(phenylmethyl)-3-pyrrolidinyl]pyridine (5.55g, 19.6 retool), a procedure analogous to that given in Example Vprovided the title compound (1.70 g, 53%) as a yellow oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.97-2.09 (1H, m), 2.11-2.40 (1H, m),2.60-2.82 (1H, m), 2.89 (1H, dt, J=10.5, 8.0, 8.0 Hz), 3.11 (1H, dd,J=10.7, 8.0 Hz), 3.18-3.29 (2H, m), 3.36-3.45 (1H, m), 4.00-4.40 (2H,m), 6.86-6.93 (2H, m), 7.87-7.90 (1H, m).

EXAMPLE Z

2-[1-(Phenylmethyl)-3-pyrrolidinyl]-3-pyridinemethanamine

Starting from 2-[1-(phenylmethyl)-3-pyrrolidinyl]-3-pyridinecarbonitrile(4.28 g, 16.3 retool), a procedure analogous to that given in Example Iprovided the title compound (4.20 g, 97%) as a yellow oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.63-1.74 (1H, m), 1.93-2.09 (1H, m),2.17-2.31 (1H, m), 2.61-2.71 (1H, m), 2.98-3.16 (1H, m), 3.22-3.34 (1H,m), 3.64-3.80 (2H, m), 3.89-3.94 (1H, m), 4.16-4.29 (2H, m), 7.07-7.12(1H, m), 7.20-7.40 (3H, m), 7.49-7.56 (1H, m), 7.58-7.66 (1H, m),7.68-7.74 (1H, m), 8.40-8.53 (1H, m).

EXAMPLE AA

2-(3-Pyrrolidinyl)-3-pyridinemethanamine

Starting from 2-[1-(phenylmethyl)-3-pyrrolidinyl]-3-pyridinemethanamine(4.10 g, 15.3 mmol), a procedure analogous to that given in Example Mprovided the title compound (1.50 g, 56%) as a yellow oil.

¹ H-NMR (300 MHz, CDCl₃): δ=1.81-1.95 (1H, m), 1.99-2.10 (1H, m), 2.30(3H, br. s), 2.79-2.89 (1H, m), 3.01-3.15 (3H, m), 3.42-3.52(1H, m),3.79 (2H, s), 6.95 (1H, dd, J=7.6, 4.8 Hz), 7.48 (1H, d, J=7.6 Hz), 8.27(1H, d, J=4.8 Hz).

PREPARATION OF SUBSTITUTED QUINOLONES AND NAPHTHYRIDONES EXAMPLE 1

7-[3-[2-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid

A suspension of7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (1.13 g, 4.0 retool), 2-(3-pyrrolidinyl)benzenemethanamine (1.25 g,5.0 mmol), and a diisopropylethylamine (2.07 g, 16.0 mmol) inacetonitrile (50 mL) was heated at gentle reflux for 24 hours. Thesuspension was allowed to cool to room temperature; the precipitatedsolids were filtered, washed successively with cold acetonitrile andether, and dried in vacuo to give the title compound (0.73 g, 43%) as awhite solid, after recrystallization from methanol, mp 226°-228° C.

¹ H-NMR (250 MHz, TFA): δ=1.21-1.38 (2H, m), 1.42-1.62 (2H, m),2.28-2.48 (1H, m), 2.50-2.76 (1H, m), 3.90-4.19 (4H, m), 4.30-4.79 (2H,m), 4.65 (2H, br. s), 7.41-7.62 (4H, m), 8.11 (1H, d, J=11.6 Hz), 9.16(1H, s), 11.60 (1H, br. s).

EXAMPLE 2

7-[3-[2-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-carboxylicacid (1.06 g, 4.0 mmol), and 2-(3-pyrrolidinyl)benzenemethanamine, aprocedure analogous to that given in Example 1 provided the titlecompound(1.08 g, 64%) as a beige solid, mp 245°-247° C.

¹ H-NMR (250 MHz, TFA): δ=1.30-1.41 (2H, m), 1.58-1.69 (2H, m),2.32-2.52 (1H, m), 2.56-2.69 (1H, m), 3.85-4.19 (5H, m), 4.21-4.40 (1H,m), 4.59-4.78 (2H, m), 7.30-7.60 (5H, m), 8.13 (1H, d, J=13.4 Hz), 9.17(1H, s), 11.63 (1H, br. s).

EXAMPLE 3

5-Amino-7-[3-[2-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (1.00 g, 4.0 retool) and 2-(3-pyrrolidinyl)benzenemethanamine, aprocedure analogous to that given in Example 1 provided the titlecompound(0.65 g, 48%) as a bright yellow solid, mp 164°-165° C.

¹ H-NMR (250 MHz, TFA): δ=1.30-1.60 (4H, m), 2.32-2.48 (1H, m),2.51-2.65 (1H, m), 3.90-4.48 (6H, m), 4.60-4.70 (2H, m), 7.43-7.61 (4H,m), 9.17 (1H, s), 11.61 (1H, br. s).

EXAMPLE 4

7-[3-[2-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-8-(trifluoromethyl)-3-quinolinecarboxylicacid

Starting from 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-8-trifluoromethyl-3-quinolinecarboxylic acid (1.00 g, 3.0 retool) and2-(3-pyrrolidinyl)benzenemethanamine, a procedure analogous to thatgiven in Example 1 provided the title compound.

¹ H-NMR (250 MHz, TFA): δ=0.97-1.14 (1H, m), 1.16-1.39 (1H, m),1.45-1.73 (2H, m), 2.10-2.75 (2H, m), 3.82-4.04 (1H, m), 4.05-4.80 (7H,m), 7.20-7.65 (4H, m), 8.07 (1H, d, J=13.4 Hz), 9.35 (1H, s).

EXAMPLE 5

7-[3-[2-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylicacid

Starting from difluoroborane1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylate(1.13 g, 3.3 mmol) and 2-(3-pyrrolidinyl)benzenemethanamine, a procedureanalogous to that given in Example 1, provided the fluoroborate ester ofthe title compound.

A suspension of the above fluoroborate ester and triethylamine (7.26 g,71.7 mmol) in ethanol-ester 10:1 (110 mL) was heated at gentle refluxfor 17 hours. The solvent was removed under reduced pressure and theresidue was chromatographed (silica gel, chloroform-methanol-ammonia75:25:5) to give the title compound (0.37 g, 73%) as a beige solid, mp170°-174° C.

¹ H-NMR (250 MHz, TFA): δ=1.20-1.36 (2H, m), 1.45-1.63 (2H, m),2.62-2.81 (2H, m), 4.05 (3H, s), 4.17- 4.61 (6H, m), 4.68 (2H, m),7.41-7.65 (4H, m), 8.32 (1H, d, J=12.0 Hz), 9.47 (1H, s), 11.62 (1H, br.s).

EXAMPLE 6

7-[3-[3-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthpyridine-3-carboxylicacid

A suspension of7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (0.85 g, 3.0 mmol),1,1-dimethyl[[3-(3-pyrrolidinyl)phenyl]methyl]carbamate (1.00 g, 3.6mmol), and diisopropylethylamine (1.55 g, 12.0 mmol) in acetonitrile (50mL) was heated at gentle reflux for 23 hours. The suspension was allowedto cool to room temperature; the precipitated solids were filtered,washedwith cold methanol, ether, and dried in vacuo at 40° C. to give1-cyclopropyl-7-[3-[3-[[(1,1-dimethylethoxy)carbonyl]amino]phenyl]-1-pyrrolidinyl]-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (1.33 g, 85%) as an off-white solid, mp 210°-211° C.

¹ H-NMR (250 MHz, d₆ -DMSO+heat): δ=1.02-1.19 (4H, m), 1.38(9H, s),2.03-2.20 (1H, m), 2.32-2.43 (1H, m), 3.42-3.98 (4H, m), 4.02-4.19(3H,m), 4.21-4.36 (1H, m), 7.13 (1H, d, J=7.1 Hz), 7.22-7.41 (4H, m),7.95(1H, d, J=12.6 Hz), 8.54 (1H, s), 15.40 (1H, br.s).

A solution of the above N-Boc protected compound (1.15 g, 2.2 mmol) and6N hydrochloric acid (20 mL) in acetone (50 mL) was heated at gentlereflux for 24 hours, and then concentrated under reduced pressure. Theresidue was dissolved in a small amount of methanol and the solutionpoured onto alarge excess of ether; the precipitated solid was filtered,washed with isopropanol and ether, and dried in vacuo at 40° C. to givethe title compound (0.94 g) as a yellow solid, mp 274°-276° C.

¹ H-NMR (250 MHz, TFA): δ=1.20-1.28 (2H, m), 1.31-1.40 (2H, m),2.23-2.54 (1H, m), 2.58-2.78 (1H, m), 3.60-3.82 (1H, m), 3.95-4.20 (3H,m), 4.35-4.78 (4H, m), 7.40-7.60 (4H, m), 8.09 (1H, d, J=11.6 Hz), 9.14(1H, s), 11.61 (1H, br. s).

EXAMPLE 7

7-[3-[3-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.80 g, 3.0 retool), a procedure analogous to that given in Example 6provided the title compound (0.98 g) as a bright yellow solid, mp250°-253° C.

¹ H-NMR (250 MHz, TFA): δ=1.32-1.45 (2H, m), 1.58-1.68 (2H, m),2.30-2.48 (1H, m), 2.57-2.73 (1H, m), 3.65-3.82 (1H, m), 3.83-4.21 (4H,m), 4.25-4.38 (1H, m), 4.46 (2H, s), 7.40-7.60 (5H, m), 8.13 (1H, d,J=13.4 Hz), 9.17 (1H, s), 11.60 (1H, br. s).

EXAMPLE 8

5-Amino-7-[3-[3-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (0.85 g, 2.5 mmol), a procedure analogous to that given in Example6provided the title compound (0.40 g) as a yellow solid afterrecrystallization from methanol-isopropanol, mp 246°-248° C.(dec).

¹ H-NMR (250 MHz, TFA): δ=1.30-1.60 (4H, m), 2.33-2.51 (1H, m),2.57-2.69 (1H, m), 3.65-3.81 (1H, m), 4.10-4.50 (7H, m), 7.42-7.60 (4H,m), 9.19 (1H, s), 11.60 (1H, br. s).

EXAMPLE 9

7-[3-[4-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid

Starting from7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (0.94 g, 3.3 mmol) and1,1-dimethylethyl[[4-(3-pyrrolidinyl)phenyl]methyl]carbamate, aprocedure analogous to that given in Example 6 provided the titlecompound (1.30 g) as an off-white solid, mp 268°-272° C.

¹ H-NMR (250 MHz, TFA): δ=1.22-1.38 (2H, m), 1.43-1.60 (2H, m),2.25-2.53 (1H, m), 2.57-2.68 (1H, m), 3.61-3.80 (1H, m), 3.97-4.20 (3H,m), 4.38-4.70 (4H, m), 7.49 (2H, d, J=7.9 Hz), 7.54 (2H, d, J=7.9 Hz),8.09 (1H, d, J=10.4 Hz), 9.15 (1H, s), 11.60 (1H, br. s).

EXAMPLE 10

7-[3-[4-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.88 g, 3.3 mmol) and1,1-dimethylethyl[[4-(3-pyrrolidinyl)phenyl]methyl]carbamate, aprocedure analogous to that given in Example 6 provided the titlecompound (1.02 g) as a bright yellow solid, mp 268°-272° C.

¹ H-NMR (250 MHz, TFA): δ=1.10-1.16 (2H, m), 1.26-1.34 (2H, m),2.14-2.25 (1H, m), 2.37-2.50 (1H, m), 3.54-3.67 (2H, m), 3.68-3.87 (3H,m), 4.00-4.10 (3H, m), 7.10 (1H, d, J=7.9 Hz), 7.48 (4H, br. s), 7.80(1H,d, J=14.0 Hz), 8.58 (1H, s), 15.32 (1H, br. s).

EXAMPLE 11

5-Amino-7-[3-[4-(aminomethyl)phenyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (0.95 g, 3.2 mmol) and1,1-dimethylethyl[[4-(3-pyrrolidinyl)phenyl]methyl]carbamate, aprocedure analogous to that given in Example 6 provided the titlecompound (0.75 g) as a yellow solid, mp 225°-227° C.

¹ H-NMR (250 MHz, TFA): δ=1.26-1.60 (4H, m), 2.27-2.48 (1H, m),2.52-2.65 (1H, m), 3.62-3.80 (1H, m), 4.11-4.50 (7H, m), 7.40-7.60 (4H,m), 9.19 (1H, s), 11.58 (1H, br. s).

EXAMPLE 12

1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[3-[3-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.93 g, 3.5 mmol) and N-methyl-3-(3-pyrrolidinyl)benzenemethanamine, aprocedure analogous to that given in Example 1 provided the titlecompound(1.38 g, 91%) as a white solid, mp 239°-240° C.

¹ H -NMR (250 MHz, TFA): δ=1.32-1.41 (2H, m), 1.58-1.67 (2H,m),2.29-2.48 (1H, m), 2.59-2.69 (1H, m), 2.99-3.05 (3H, m), 3.61-3.79(1H, m),3.81-4.20 (4H, m), 4.25-4.44 (3H, m), 7.32-7.59 (5H, m), 8.12(1H, d, J=l 3.4 Hz), 9.16 (1H, s), 11.63 (1H, br. s).

EXAMPLE 13

5-Amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-[3-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (0.52 g, 1.7 mmol) andN-methyl-3-(3-pyrrolidinyl)benzenemethanamine, a procedure analogous tothat given in Example 1 provided the title compound (0.44 g, 55%) as ayellow solid, mp >270° C.

¹ H-NMR (250 MHz, TFA): δ=1.25-1.62 (4H, m), 2.30-2.49 (1H, m),2.52-2.69 (1H, m), 2.99-3.07 (3H, m), 3.65-3.90 (1H, m), 4.10-4.45 (7H,m), 7.40-7.60 (4H, m), 9.26 (1H, s), 11.58 (1H, br. s).

EXAMPLE 14

1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[3-[4-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.80 g, 3.0 mmol) and N-methyl-4-(3-pyrrolidinyl)benzenemethanamine, aprocedure analogous to that given in Example 1 provided the titlecompound(1.11 g, 85%) as an off-white solid, mp 235°-237° C.

¹ H-NMR (250 MHz, TFA): δ=1.33-1.39 (2H, m), 1.58-1.64 (2H, m),2.30-2.47 (1H, m), 2.58-2.68 (1H, m), 3.00-3.05 (3H, m), 3.68-3.79 (1H,m), 3.81-4.20 (4H, m), 4.23-4.41 (3H, m), 7.20-7.40 (1H, m), 7.51 (4H,br.s), 8.12 (1H, br. d, J=13.4 Hz), 9.16 (1H, s), 11.65 (1H, br. s).

EXAMPLE 15

5-Amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-[3-[4-[(methylamino)methyl]phenyl]-1-pyrrolidinyl]-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (0.89 g, 3.0 mmol) and N-methyl-4-(3-pyrrolidinyl)benzenemethanamine, a procedure analogous to that given in Example 1provided the title compound (0.71 g, 51%) as a yellow solid, mp201°-205° C.

¹ H-NMR (250 MHz, TFA): δ=1.30-1.39 (2H, m), 1.45-1.54 (2H, m),2.28-2.47 (1H, m), 2.53-2.68 (1H, m), 2.99-3.06 (3H, m), 3.68-3.80 (1H,m), 4.08-4.40 (7H, m), 7.22-7.40 (1H, m), 7.52 (4H, br. s), 9.17 (1H,s), 11.62 (1H, br. s).

EXAMPLE 16

¹-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid

Starting from7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (1.33 g, 4.7 mmol) and 2-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound (1.64g, 88%) as an off-white solid, mp 203°-204° C.

¹ H-NMR (250 MHz, TFA): δ=1.22-1.38 (2H, m), 1.42-1.60 (2H, m),2.47-2.73 (1H, m), 2.82-3.00 (1H, m), 4.01-4.64 (5H, m), 4.70-5.00 (1H,m), 8.05-8.28 (3H, m), 8.72 (1H, dist. t, J=7.9 Hz), 8.84 (1H, br. d,J=5.5 Hz), 9.20 (1H, s), 11.71 (1H, br. s).

EXAMPLE 17

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidnyl]-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(1.25 g, 4.7 retool) and 2-(3-pyrrolidinyl)pyridine, a procedureanalogousto that given in Example 1 provided the title compound (1.57 g,85%) as an off-white solid, mp 216°-219° C.

¹ H-NMR (250 MHz, TFA): δ=1.38-1.46 (2H, m), 1.60-1.69 (2H, m),2.50-2.70 (1H, m), 2.82-2.98 (1H, m), 3.94-4.32 (5H, m), 4.50-4.67 (1H,m), 7.44 (1H, d, J=7.0 Hz), 8.06-8.23 (3H, m), 8.72 (1H, t, J=7.9 Hz),8.83 (1H, d, J=5.4 Hz), 9.21 (1H, s), 11.65 (1H, br. s).

EXAMPLE 18

5-Amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid

Starting from 5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (0.97 g, 2.9 mmol) and2-(3-pyrrolidinyl)pyridine, a procedure analogous to that given inExample1 provided the title compound (1.12 g, 91%) as a bright yellowsolid, mp 206°-208° C.

¹ H-NMR (250 MHz, TFA): δ=1.21-1.38 (2H, m), 1.40-1.52 (2H, m),2.41-2.60 (1H, m), 2.75-2.89 (1H, m), 4.07-4.38 (5H, m), 4.43-4.57 (1H,m), 8.07-8.13 (1H, m), 8.20 (1H, d, J=7.9 Hz), 8.70 (1H, dist. t, J=7.9Hz), 8.80 (1H, d, J=5.6 Hz), 9.14 (1H, s), 11.65 (1H, br. s).

EXAMPLE 19

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyridinyl)-1-pyrrolidinyl]-8-(trifluoromethyl)-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-8-trifluoromethyl-3-quinolinecarboxylicacid (1.33 g, 4.0 retool) and 2-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound(1.36 g,74%) as a yellow solid, mp 210°-212° C.

¹ H-NMR (250 MHz, TFA): δ=0.98-1.11 (1H, m), 1.13-1.27 (1H, m),1.43-1.70 (2H, m), 2.45-2.70 (1H, m), 2.81-2.97 (1H, m), 4.12-4.60 (6H,m), 8.05-8.29 (3H, m), 8.63-8.78 (1H, m), 8.86 (1H, dist. d, J=6.0 Hz),9.40 (1H, s), 11.60 (1H, br. s).

EXAMPLE 20

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid

Starting from7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (1.24 g, 4.4 retool) and 3-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound(1.43 g,82%) as a light beige solid, mp 226°-228° C.

¹ H-NMR (250 MHz, TFA): δ=1.20-1.38 (2H, m), 1.42-1.60 (2H, m),2.36-2.60 (1H, m), 2.74-2.90 (1H, m), 3.95-4.90 (6H, m), 8.09-8.22 (2H,m), 8.76 (1H, d, J=8.3 Hz), 8.82 (1H, d, J=5.8 Hz), 8.97 (1H, s), 9.17(1H, s), 11.62 (1H, br. s).

EXAMPLE 21

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(1.06 g, 4.0 mmol) and 3-(3-pyrrolidinyl)pyridine, a procedure analogousto that given in Example 1 provided the title compound (1.15 g, 73%) asanoff-white solid, mp 233°-236° C.

¹ H-NMR (250 MHz, TFA) δ=1.35-1.42 (2H, m), 1.59-1.68 (2H, m), 2.39-2.57(1H, m), 2.72-2.86 (1H, m), 3.92-4.23 (5H, m), 4.47-4.58 (1H, m), 7.42(1H, d, J=7.1Hz), 8.15-8.25 (2H, m), 8.78 (1H, d, J=8.4 Hz), 8.84(1H, d,J=5.8 Hz), 8.98 (1H, br. s), 9.20 (1H, s), 11.63 (1H, br. s).

EXAMPLE 22

5-Amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (1.04 g, 3.5 retool) and 3-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound (1.26g, 84%) as a yellow solid, mp 250°-252° C.

¹ H-NMR (250 MHz, TFA): δ=1.22-1.56 (4H, m), 2.28-2.47 (1H, m),2.65-2.79 (1H, m), 3.85-4.00 (1H, m), 4.16-4.52 (5H, m), 8.17 (1H, dd,J=8.1, 5.8 Hz), 8.73 (1H, d, J=8.2 Hz), 8.80 (1H, d, J=5.8 Hz), 8.93(1H, s), 9.12 (1H, s), 11.65 (1H, br. s).

EXAMPLE 23

1-Cyclopropyl,6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid

Starting from7-chloro-l-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (0.85 g, 3.0 mmol) and 4-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound (0.79g, 67%), mp 223°-225° C.

¹ H-NMR (300 MHz, TFA): δ=1.03-1.12 (2H, m), 1.13-1.24 (2H, m),2.18-2.28 (1H, m), 2.47-2.60 (1H, m), 3.62-3.76 (1H, m), 3.84-4.00 (3H,m), 4.05-4.18 (1H, m), 4.36-4.44 (1H, m), 8.02 (1H, d, J=12.5 Hz), 8.14(2H, d, J=5.7 Hz), 8.59 (1H, s), 8.92 (2H, d, J=5.7 Hz), 12.12 (1H, br.s).

EXAMPLE 24

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(1.13 g, 4.3 mmol) and 4 -(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound (0.87g, 52%) as anoff-white solid, mp 260°-261° C.

¹ H-NMR (250 MHz, TFA): δ=1.38-1.47 (2H, m), 1.52-1.72 (2H, m),2.40-2.60 (1H, m), 2.79-2.94 (1H, m), 3.94-4.20 (5H, m), 4.47-4.63 (1H,m), 7.43 (1H, d, J=7.9 Hz), 8.14-8.21 (3H, m), 8.86 (2H, d, J=5.2 Hz),9.21(1H, s), 11.65 (1H, br. s).

EXAMPLE 25

5-Amino-1-cyclopropyl,6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid

Starting from 5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (1.10 g, 3.7 mmol) and4-(3-pyrrolidinyl)pyridine, a procedure analogous to that given inExample1 provided the title compound (0.75 g, 48%) as a yellow solid, mp236°-238° C.

¹ H-NMR (250 MHz, TFA): δ=1.22-1.38 (2H, m), 1.41-1.57 (2H, m),2.32-2.47 (1H, m), 2.66-2.81 (1H, m), 3.90-4.07 (1H, m), 4.18-4.38 (4H,m), 4.41-4.50 (1H, m), 8.18 (2H, d, J=6.4 Hz), 8.85 (2H, d, J=6.3 Hz),9.15 (1H, s), 11.62 (1H, br. s).

EXAMPLE 26

1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-8-(trifluoromethyl)-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-8-trifluoromethyl-3-quinolinecarboxylicacid (1.05 g, 3.5 mmol) and 4-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1 provided the title compound(0.93 g,58%) as a beige solid, mp 244°-245° C.

¹ H-NMR (250 MHz, TFA): δ=0.99-1.18 (1H, m), 1.19-1.35 (1H, m),1.43-1.74 (2H, m), 2.37-2.60 (1H, m), 2.75-2.89 (1H, m), 3.98-4.62 (6H,m), 8.08-8.27 (3H, m), 8.81-8.93 (2H, m), 9.39 (1H, s), 11.63 (1H, br.s).

EXAMPLE 27

7-[3-(3-Amino-2-pyridinyl)-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.81 g, 3.1 mmol) and 2-(3-pyrrolidinyl)-3-pyridinamine, a procedureanalogous to that given in Example 1 provided the title compound (1.15g, 91%) as an off-white solid, mp >270° C.

¹ H-NMR (250 MHz, TFA): δ=1.36-1.47 (2H, m), 1.59-1.69 (2H, m),2.58-2.71 (1H, m), 2.73-2.88 (1H, m), 3.96-4.30 (5H, m), 4.42-4.60 (1H,m), 7.46 (1H, d, J=6.9 Hz), 7.76 (1H, dd, J=8.5, 5.6 Hz), 7.99 (1H, d,J=8.5 Hz), 8.13 (1H, d, J=5.5 Hz), 8.19 (1H, d, J=13.3 Hz), 9.22 (1H,s), 11.63 (1H, br. s).

EXAMPLE 28

7-[3-[3-(Aminomethyl)-2-pyridinyl]-1-pyrrolidinyl]-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid(0.80 g, 3.0 mmol) and 2-(3-pyrrolidinyl)-3-pyridinemethanamine, aprocedure analogous to that given in Example 1 provided the titlecompound(1.09 g, 86%) as an off-white solid, mp 246°-248° C.

¹ H-NMR (250 MHz, TFA): δ=1.37-1.45 (2H, m), 1.60-1.68 (2H, m),2.63-2.80 (1H, m), 2.82-3.00 (1H, m), 3.96-4.14 (2H, m), 4.18-4.29 (1H,m), 4.31-4.40 (1H, m), 4.50-4.70 (2H, m), 5.03 (2H, m), 7.47 (1H, d,J=6.9Hz), 8.14-8.22 (2H, m), 8.97-9.04 (2H, m), 9.23 (1H, s), 11.65 (1H,br. s).

EXAMPLE 29

5-Amino-7-[3-[3-(aminomethyl)-2-pyridinyl]-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid

Starting from5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylicacid (0.60 g, 2.0 retool) and 2-(3-pyrrolidinyl)-3-pyridinemethanamine,aprocedure analogous to that given in Example 1 provided the titlecompound (0.74 g, 81%) as a yellow solid, mp 226°-228° C.

¹ H-NMR (250 MHz, TFA): δ=1.25-1.38 (2H, m), 1.41-1.57 (2H, m),2.50-2.72 (1H, m), 2.75-2.90 (1H, m), 4.19-4.39 (3H, m), 4.41-4.60 (3H,m), 5.01 (2H, br. s), 8.17 (1H, dd, J=7.6, 6.3 Hz), 8.93-9.03 (2H, m),9.15 (1H, s), 11.64 (1H, br. s).

EXAMPLE 30

7-[3-[2-(Aminomethyl)phenyl]-1-pyrrolidinyl]-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylicacid

Starting from6,7-difluoro-1-(2,4-difluorophenyl)-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylicacid (0.40 g, 1.1 retool) and 2-(3-pyrrolidinyl)benzenemethanamine, aprocedure analogous to that given in Example 1, provided the titlecompound (0.40 g, 72%) as a beige solid, mp 283°-285° C. (dec).

¹ H-NMR (250 MHz, TFA): δ=2.14-2.30 (1H, m), 2.41-2.59 (1H, m), 2.96(3H, s), 3.65-3.97 (4H, m), 4.04-4.22 (1H, m), 4.47-4.68 (2H, m),7.21-7.60 (6H, m), 62-7.78 (1H, m), 8.98 (1H, s), 11.65 (1, br. s).

EXAMPLE 31

1-(2,4-Difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylicacid

Starting from7-chloro-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylicacid (0.51 g, 1.5 mmol) and 4-(3-pyrrolidinyl)pyridine, a procedureanalogous to that given in Example 1, provided the title compound (0.39g, 56%) as an off-white solid, mp 253°-255° C. (dec).

¹ H-NMR (300 MHz, d₆ -DMSO): δ=1.88-2.10 (1H, m), 2.21-2.40(1H, m),3.20-3.60 (5H, m), 7.23-7.39 (3H, m), 7.57-7.68 (1H, m), 7.82 (1H,td,J=8.7, 6.0 Hz), 8.10 (1H, d, J=12.6 Hz), 8.51 (2H, d, J=6.0 Hz), 8.83(1H, s), 15.18 (1H, br. s).

EXAMPLE 32

3-[1-(3-Carboxy-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-quinolyl)-3-pyrrolidinyl]-1-methylpyridiniumiodide

Iodomethane (1.62 g, 11.4 mmol) was added dropwise to a stirredsuspension of1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(3-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid (0.30 g, 0.8 mmol) in acetonitrile (30 mL). The resulting mixturewas heated at reflux for 2 hours. The suspension wasthen filtered, thesolids were washed with acetonitrile and ether, and dried in vacuo at40° C. to give the title compound (0.38 g, 88%) as a light yellow solid,mp 278°-280° C.

¹ H-NMR (250 MHz, d₆ -DMSO): δ=1.10-1.20 (2H, m), 1.27-1.38(2H, m),2.16-2.39 (1H, m), 2.47-2.60 (1H, m), 1.27-1.38 (2H, m), 2.16-2.39(1H,m), 2.47-2.60 (1H, m), 3.66-3.95 (5H, m), 4.05-4.18 (1H, m), 4.38 (3H,s), 7.08-7.17 (1H, m), 7.78 (1H, d, J=14.1 Hz), 8.15 (1H, dist. t,J=6.6, 7.3 Hz), 8.55 (1H, s), 8.65 (1H, br. d, J=7.9 Hz), 8.93 (1H, d,J=5.7 Hz), 9.13 (1H, s), 15.42 (1H, br. s).

EXAMPLE 33

4-[1-(3-Carboxy-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-quinolyl)-3-pyrrolidinyl]-1-methylpyridiniumiodide

Starting from1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(4-pyridinyl)-1-pyrrolidinyl]-3-quinolinecarboxylicacid (0.40 g, 1.0 retool), a procedure analogous tothat given in Example32, provided the title compound (0.50 g, 93%) as a light yellow solid,mp >280° C.

¹ H-NMR (300 MHz, d₆ -DMSO): δ=1.12-1.18 (2H, m), 1.23-1.39(2H, m),2.17-2.28 (1H, m), 2.50-2.60 (1H, m), 3.70-3.98 (5H, m), 4.10-4.20(1H,m), 4.32 (3H, s), 7.16 (1H, d, J=7.9 Hz), 7.85 (1H, d, J=14.3 Hz), 8.17(2H, d, J=6.7 Hz), 8.60 (1H, s), 8.95 (2H, d, J=6.6 Hz), 15.47 (1H, br.s).

We claim:
 1. A compound of the formula ##STR8## wherein * denotes an asymmetric carbon;X is C--H, C--F, C--Cl, C--OCH₃, C--CF₃, or N; R¹ is a C₁ -C₄ -alkyl, C₃ -C₆ -cycloalkyl, or phenyl substituted by one or more halogen atoms; R² is a hydrogen, alkyl of 1 to 4 carbon atoms, or a cation; R³ is hydrogen, amino, or methyl; V, W, Y, and Z are each independently C--H, or nitrogen; T is C--H or nitrogen; n is 1-; R⁴ is hydrogen or one, two or three substituents independently selected from C₁ -C₄ -alkyl, halo-substituted C₁ -C₄ -alkyl, hydroxy-substituted C₁ -C₄ -alkyl, halogen, hydroxy, C₁ -C₄ -alkoxy, mercapto, amino, mono-(C₁ -C₄ -alkyl)amino, di-(C₁ -C₄ -alkyl)amino, formamido, mono-(C₁ -C₄ -alkyl)amido, di-(C₁ -C₄ -alkyl)amido, cyano, nitro, C₁ -C₄ -alkoxycarbonyl, carboxyl, aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl, di-(C₁ -C₄ -alkyl) aminomethyl, wherein free hydroxy and amino groups may be protected; with the proviso that when T, V, W, Y, and Z are C--H and n is 1, R₄ is aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl or di-(C₁ -C₄ -alkyl)aminomethyl,or a pharmaceutically acceptable acid addition or quaternery ammonium salt thereof; ##STR9##
 2. A compound according to claim 1, wherein R¹ is C₃ -C₆ -cycloalkyl or phenyl substituted by one or more halogen atoms, and R⁴ is hydrogen, hydroxy, C₁ -C₄ -alkoxy, hydroxy substituted C₁ -C₄ -alkyl, amino, mono-(C₁ -C₄ -alkyl)amino, di-(C₁ -C₄ -alkyl)amino, aminomethyl, mono-(C₁ -C₄ -alkyl)aminomethyl, or di-(C₁ -C₄ -alkyl)aminomethyl.
 3. A compound according to claim 2 wherein X is C--H, C--F, C--Cl, C--OCH₃, or N; R¹ is cyclopropyl or 2,4-difluorophenyl; R³ is hydrogen or amino, and R⁴ is hydrogen, hydroxy, hydroxymethyl, amino, methylamino, dimethylamino, aminomethyl, methylaminomethyl, or dimethylaminomethyl.
 4. A compound according to claim 3 wherein R² is hydrogen or a cation, and R⁴ is hydrogen, hydroxy, hydroxymethyl, amino, or aminomethyl.
 5. A compound according to claim 3 wherein the combination of T, V, W, Y, and Z is a heteroaromatic ring selected from the group consisting of 3- and 4-pyridazinyl, 2-, 4-, and 5-pyrimidinyl, and 2-pyrazinyl.
 6. A compound according to claim 5 wherein R₂ is hydrogen or a cation, and R⁴ is hydrogen, hydroxy, hydroxymethyl, amino, or aminomethyl.
 7. A compound according to claim 1 and being 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(2-pyrimidinyl)-1-pyrrolidinyl]-1,8-naphthyridine-3-carboxylic acid.
 8. A compound according to claim 1 and being 1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-7-[3-(4-pyrimidinyl)-1-pyrrolidinyl]-3-quinolinecarboxylic acid.
 9. A compound according to claim 1 and being 5-amino-1-cyclopropyl-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-7-[3-(2-pyrazinyl)-1-pyrrolidinyl]-3-quinolinecarboxylic acid.
 10. A pharmaceutical composition comprising an antibacterially effective amount of a compound as claimed in claim 1 together with a pharmaceutically acceptable carrier.
 11. A method of treating bacterial infections in mammals which comprises administering to said mammal a pharmaceutical composition as claimed in claim 10 in unit dosage form. 